For vape shops, there is finally good news from the FDA!

By vapesmoant

The US Food and Drug Administration will allow vape stores to change coils, assembly vape kits, and refill nebulizers for customers on site, even if they are not designated as tobacco product manufacturers under presumptive rules.
The federal agency has just issued guidelines for the rules, for the first time in plain English what activities are allowed in retail stores. Since the presumption regulations were announced, business owners have repeatedly tried to make clarifications.

The presumption rule was issued in May last year and became effective on August 8, 2016. According to the FDA, any retail company that “creates or modifies” newly identified “tobacco products” (including all Vape and vapor products) will be regarded as a manufacturer and needs to be registered as a manufacturer and list all the products they sell , Submit health documents to the agency, report a list of ingredients, and report harmful and potentially harmful ingredients (HPHC). steam crave In addition, manufacturers need to submit a pre-market tobacco application (PMTA) for all products they create or modify.
Many vapor retailers have explained these regulations, including prohibiting basic customer service activities such as changing coils, assembling equipment for a new Vape smoker’s kit, simple repairs, or explaining product features. The FDA has avoided specifying exactly what is allowed in several online seminars, phone calls, and emails with shop owners.
The following activities can be carried out without the vape shop being certified as a manufacturer:
· “Demonstrate or explain timesvape the use of ENDS products (Electronic Nicotine Delivery System) without assembling the product”
· “Maintain ENDS products by cleaning or tightening fixing devices (such as screws)”
· “Replace the coil in the ENDS product with the same coil (for example, the same resistance and rated power)”
· “Assemble components and parts into the final product in the ENDS kit”
In addition, the FDA  stated that it apv mods will not enforce some activities that are deemed “modified” product categories. According to its announcement, the FDA “does not intend to enforce the five requirements listed above on these vape stores, if, in general, all modifications are consistent with the FDA’s marketing authorization (MA) conditions, or the original manufacturer The specifications provided and all modifications made are consistent with these specifications.”
Examples of modifications currently allowed by the FDA include:
· “Refill an open ENDS system, if before, during and after filling, the equipment or e-liquid is not further modified beyond the FDA marketing authorization (MA) order”
·”Refill an open ENDS system, if further modifications to the equipment and e-liquid before, during and after filling are not inconsistent with the manufacturer’s specifications, if there is no MA command
In other words, they will allow the store to help customers refill the atomizer as long as they do not make any modifications to the equipment other than what the manufacturer recommends (with marketing orders or instructions).
They specifically explained that it is forbidden to replace any coils other than spare coils designed for specific atomizers. Therefore, it is not allowed to be made by shop assistants for customers. Filling closed system equipment is also prohibited smoant.
The publication of the new draft guidelines also opened a simple window for public comments. All retailers and customers of adv vape stores can make specific criticisms or suggestions about how the presumption rules affect vape store transactions.
The draft guidance closely follows the two manufacturer-related deadlines postponed by the FDA. The deadline for manufacturers to register with the agency has been postponed from December 31, 2016 to June 30, 2017. Soon after, the FDA also postponed the deadline for submitting the ingredient list from February 8 to August 8, 2017.
Finally, the agency announced in this document that it will not force all tobacco products to show “an accurate description of the percentage of foreign and domestic tobacco used in the product.” It is really comforting.